참고문헌
- Badr, M. Z. A, Mahgoub, S. A, Atla, F. M., and Moustafa, O. S., Chemistry and Cyclization Reactions of Pyrimidothienoquinoxaline Derivatives. Part-IV. J. Indian Chem. Soc., 74, 30-32 (1997)
- Campaigne, E. and Mclaughin, A R, Some Sulfur-containing Quinoxalines. J. Heterocyclic Chem., 20, 623-628 (1983) https://doi.org/10.1002/jhet.5570200323
- Campaigne, E. and Mclaughlin, A. R., Some 4-Alkyl s-Triazolo [4,3-a]quinoxalines. J. Heterocyclic Chem., 20, 781-782 (1983) https://doi.org/10.1002/jhet.5570200354
- Campiani, G. Aiello, F., Fabbrini, M. Morelli, E. Ramunno, A. Armaroli, S. Nacci, V. Garofalo, A. Greco, G. Novellino, E. Maga, G. Spadari, S. Bergamini, A. Ventura, L. Bongiovanni, B. Capozzi, M. Bolacchi, F. Marini, S. Coletta, M. Guiso, G., and Caccia, S., Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agent. J. Med. Chem., 44, 305-315 (2001) ㈀ 硯⨀ 灯⨀ 䢤⨀ က 렋 ⨀ ⨀ 視⨀ 탡ヨ⨀ က 塢⨀ 偢⨀ 婢⨀ 룥ヨ⨀ က က 䡣⨀ 䁣⨀ 䩣⨀ 飪ヨ⨀ က 䀀 롢⨀ 끢⨀ 멢⨀ ヨ⨀ က ⡢⨀ ⨀ ⩢⨀ ヨ⨀ က 塥⨀ 健⨀ ᣫヨ⨀ ᠀ https://doi.org/10.1021/jm0010365
- Cheesman, G. W. H. and Rafiq, M., Quinoxaline and related compounds part VIII; Reactions of quinoxaline-2-(1H)ones and 2,3-(1H,4H)diones with hydrazines. J. Chem. Soc., (C), 452-456 (1971)
- Collins, C. H. Microbiological Methods. Butterworths, London, pp. 92, (1964)
- Dirlam, J. P., Presslitz, J. E., and Williams, B. J., Synthesis and antibacterial activity of some 3-[(alkylthio)methyl]quinoxaline 1-oxide derivatives. J. Med. Chem., 26, 1122-1126 (1983) https://doi.org/10.1021/jm00362a007
- El-Hawash, S. A., Habib, N. S., and Fanaki, N. H., Quinoxaline derivatives part II: Synthesis and antimicrobial testing of 1,2,4-triazolo[4,3-a]quinoxalines, 1,2,4-triazino[4,3-a]quinoxalines and 2-pyrazolylquinoxalines. Pharmazie, 54, 808-815 (1999)
- Krishnan, V. S. H., Narayan, G. K. A. S. S., Reddy-Sastry, C. V., Vemana, K., Trivedi, B. S., and Rao, B. E., Reaction of 3hydrazinoquinoxaline- 2-(1H)one with aromatic carbocyclic acids using diphenylphosphoryl azide: synthesis and antiallergic activity of s-triazolo[4,3-a]quionxaline-4-ones. Indian. J. Heterocyclic Chem., 3, 227-237 (1994)
- Kurasawa, Y., Muramatsu, M., Yamazaki, K., Okamoto, Y., and Takada, A, Synthesis of 3-(a-Chlorophenylhydrazono)heteroarylmethyl-2-oxo-1,2-dihydroquinoxalines with Antimicrobial Activity. J. Heterocyclic Chem., 23, 1387-1390 (1986) https://doi.org/10.1002/jhet.5570230526
- Rashed, N., El-Massry, A., El-Ashry, E. H., Amer, A., and Zimmer, H., A Facile Synthesis of Novel Triazoloquinoxalinones and Triazinoquinoxalinones. J. Heterocyclic Chem., 27, 691-694 (1990) https://doi.org/10.1002/jhet.5570270339
- Reddy-Sastry, C. V., Marwah, P., Marwah, A. K., and Rao, G.S., Synthesis and biological activity of some new N-arylcarbamoyl and arylthiocarbamoyl hydrazinoquinoxalin-2-ones. Indian. J. Chem., 28B, 885-891 (1989)
- Reddy-Sastry, C. V, Srinivasa-Rao, K., Krishnan, V. S. H., Rastogi, K., Jain, M. L., and Narayan, G. K. A. S. S., Synthesis and biological activity of some new tetrazolo-benzoxazines and bis-tetrazoloqinoxalines. Indian J. Chem., 29B, 396-403 (1990)
- Sarges, R., Howard, H. R., Browne, R. G., Lebel, L. A., Seymour, P. A., and Koe, B. K., 4-Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants. J. Med. Chem., 33, 2240-2254 (1990) https://doi.org/10.1021/jm00170a031
- Trivedi, B. K. and Bruns, R. F., [1,2,4]Triazolo[4,3-a]quinoxalin-4-amines: a new class of A1 receptor selective adenosine antagonists. J. Med. Chem., 31, 1011-1014 (1988) https://doi.org/10.1021/jm00400a021
- Vierfond, J. M., Legendre, L., Martin, C., Rinjard, P., and Miocque, M., Thieno- and isothiazolo(3,4-b)quinoxalines: synthesis, structure and pharmacological study. Eur. J. Med. Chem. Chim. Ther., 25, 251-255 (1990) https://doi.org/10.1016/0223-5234(90)90208-K
- Yoo, H. W., Suh, M. E., and Park, S. W., Synthesis and cytotoxicity of 2-methyl-4, 9-dihydro-1-substituted-1H-imidazo[4,5-g]quinoxaline-4,9-diones and 2,3-disubstituted-5,10-pyrazino[2,3-g]quinoxalinediones. J. Med. Chem., 41, 4716-4722 (1998) https://doi.org/10.1021/jm970695n
-
Youssef, A. F., Farag, H. H., Abdel-kader, M. A., and El-Gendy, M. A., Unsymetrical N,N-disubstituted anilines; Synthesis of
$\alpha$ (n-methylanilino)acetamide. Indian J. Chem., 14B, 279-286 (1976)